FDA 510(k)
Substantially Equivalent
🇺🇸 United States
PATIENT MONITORING SYSTEM
K Number: K760559
·
Decision Sep 10, 1976
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
254
Review Days
8
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- PATIENT MONITORING SYSTEM
- K Number
- K760559
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- General Electric Co.
- Date Received
- September 2, 1976
- Decision Date
- September 10, 1976
- Advisory Committee
- Unknown
- Review Advisory Committee
- CV
- Third Party
- N
Other Clearances by General Electric Co.
| K Number | Device Name | ||
|---|---|---|---|
| K103489 | GE VEO RECONSTRUCTION OPTION | Sep 9, 2011 | Substantially Equivalent |
| K082317 | GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTION | Sep 26, 2008 | Substantially Equivalent |
| K081921 | GE VIVID E9 ULTRASOUND | Aug 6, 2008 | Substantially Equivalent |
| K073297 | GE LOGIQ P6 | Dec 18, 2007 | Substantially Equivalent |
| K072952 | GE ECHOPAC | Nov 16, 2007 | Substantially Equivalent |
| K072797 | GE LOGIQ I COMAPACT ULTRASOUND, GE LOGIQ E COMPACT ULTRASOUND, GE VIVID E COMPACT ULTRASOUND | Oct 17, 2007 | Substantially Equivalent |
| K072075 | MODIFICATION TO GE LOGIQ A3 | Aug 29, 2007 | Substantially Equivalent |
| K071985 | GE VIVID S5 AND S6 DIAGNOSTIC ULTRASOUND | Aug 17, 2007 | Substantially Equivalent |
| K063006 | GE LOGIQ WORKS | Nov 2, 2006 | Substantially Equivalent |
| K061682 | GE VOLUSON E8 ULTRASOUND SYSTEM | Jul 12, 2006 | Substantially Equivalent |